High Throughput Screening Assay for the TRPM5 Ion Channel

ABSTRACT

There exists a need in the art for high throughput screening assays that can identify compounds that specifically modulate the activity of fast-acting ion channels, such as TRPM5. Current methods suffer from a lack of sensitivity, low throughput, and are labor intensive. The claimed methods provide fluorescent assays with an optical readout that gives rapid readout of the results, has a high signal to noise background ratio, are easy to use, can be modified for automation and miniaturization, and provide verification that a compound specifically modulates TRPM5.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. Non-Prov. Appl. No. 11/592,180,filed Nov. 3, 2006, which claims the benefit of U.S. Prov. Appl. No.60/732,636, filed Nov. 3, 2005, which is herein incorporated byreference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention is related to a high throughput screening methodfor compounds that impact taste. More specifically, the presentinvention relates to a screening method useful in the identification ofcompounds that affect taste sensation by modulating the activity of theion channel TRPM5. The screening method, using fluorescent membranepotential dyes, allows for the rapid screening of thousands of compoundsby providing a visual fluorescent readout that can be easily automated.

2. Background

Taste perception not only plays a critical role in the nutritionalstatus of human beings, but is also essential for the survival of bothlower and higher animals (Margolskee, R. F. J. Biol. Chem. 277:1-4(2002); Avenet, P. and Lindemann, B. J. Membrane Biol. 112:1-8 (1989)).Taste perception is carried out by taste receptor cells (TRCs). TRCsperceive the multitude of compounds that are associated with a giventaste, and convert that perception to a signal deciphered by the brain,resulting in sweet, bitter, sour, salty, or umami (savory) taste.

TRCs are polarized epithelial cells, meaning they have specializedapical and basolateral membranes. Taste buds contain 60-100 TRCs, eachhaving a tiny portion of its membrane exposed on the mucosal surface ofthe tongue (Kinnamon, S. C. TINS 11:491-496 (1988)). Sensorytransduction is initiated by sapid molecules, or “tastants,” thatinteract with microvillar processes on the apical membrane of TRCs. Thetastants bind specific membrane receptors, leading to a voltage changeacross the cell membrane; in turn this depolarizes, or changes theelectric potential of the cell, causing transmitter release andexcitation of primary gustatory nerve fibers.

Ion channels are transmembrane proteins that form pores in a membraneand allow ions to pass from one side to the other (reviewed in B. Hille(Ed), 1992, Ionic Channels of Excitable Membranes 2nd ed., Sinauer,Sunderland, Mass.). Although certain ion channels are open under allphysiological membrane conditions (so-called leaky channels), manychannels have “gates” that open in response to a specific stimulus. Asexamples, voltage-gated channels respond to a change in the electricpotential across the membrane, mechanically-gated channels respond tomechanical stimulation of the membrane, and ligand-gated channelsrespond to the binding of specific molecules. Various ligand-gatedchannels can open in response to extracellular factors, such as aneurotransmitters (transmitter-gated channels), or intracellularfactors, such as ions (ion-gated channels), or nucleotides(nucleotide-gated channels). Still other ion channels are modulated byinteractions with proteins, such as G-proteins (G-protein coupledreceptors or GPCRs).

Most ion channel proteins mediate the permeation of one predominantionic species. For example, sodium (Na⁺), potassium (K⁺), chloride(Cl⁻), and calcium (Ca²⁺) channels have been identified.

One recently discovered ion channel, TRPM5, has been shown to beessential for taste transduction. Perez et al., Nature Neuroscience5:1169-1176 (2002); Zhang et al., Cell 112:293-301 (2003). TRPM5 is amember of the transient receptor potential (TRP) family of ion channels.TRPM5 forms a channel through the membrane of the taste receptor cell,and is believed to be activated by stimulation of a receptor pathwaycoupled to phospholipase C and by IP₃-mediated Ca²⁺ release. The openingof this channel is dependent on a rise in Ca²⁺ levels. Hofmann et al.,Current Biol. 13:1153-1158 (2003). The activation of this channel leadsto depolarization of the TRC, which in turn leads to transmitter releaseand excitation of primary gustatory nerve fibers.

Because TRPM5 is a necessary part of the taste-perception machinery, itsinhibition prevents an animal from sensing particular tastes. Althoughtaste perception is a vital function, the inhibition, or masking, ofundesirable tastes is beneficial under certain circumstances. Forexample, many active pharmaceutical ingredients of medicines produceundesirable tastes, such as a bitter taste. Inhibition of the bittertaste produced by the medicine may lead to improved acceptance by thepatient. In other circumstances, enhancement of taste may be desirableas in the case of developing improved artificial sweeteners or intreatment of taste losses in groups such as the elderly. Mojet et al.,Chem Senses 26:845-60 (2001).

TRPM5 displays voltage modulation and rapid activation/deactivation(“opening and closing”) kinetics upon receptor stimulation (Hofmann etal. 2003) which allows for the passage of monovalent cations, such assodium and potassium. A closely related protein, TRPM4b, also shows Ca²⁺dependent voltage modulation, but opens and closes much slower thanTRPM5. Thus, TRPM5 is the first example of a voltage-modulated,Ca²⁺-activated, monovalent cation channel that has rapidactivation/deactivation kinetics (Hofmann et al. 2003).

Ion channel activation or inhibition may be determined by measuringchanges in cell membrane potential when cells are exposed to certainstimuli. This is an indirect method of evaluating ion channelmodulation, as cell membrane potential may be affected by multiplechannels.

One method for testing ion channel activity is to measure changes incell membrane potential using the patch-clamp technique. (Hamill et al.,Nature 294:462-4 (1981)). In this technique, a cell is attached to anelectrode containing a micropipette tip which directly measures theelectrical conditions of the cell. This allows detailed biophysicalcharacterization of changes in membrane potential in response to variousstimuli. Thus, the patch-clamp technique can be used as a screening toolto identify compounds that modulate activity of ion channels. However,this technique is difficult to master and requires significant expertiseto generate consistent, reliable data. Moreover, this technique is timeconsuming and would allow fewer than two or three compounds per day tobe screened for activity.

Ideally, methods of screening test compounds are high throughput (i.e.,allow for many compounds to be screened quickly), automated, easy touse, sensitive, and selective. Screening assays should also provide ahigh signal to background noise ratio. (Baxter et al., J. Biomol.Screen. 7:79-85 (2002)). Background noise is the minimal stimulationthat a compound produces regardless of its effect on the ion channel.The high ratio makes visualization of positive or negative modulatorssimpler because the smallest response will be seen over the backgroundmeasurements. This leads to a clear identification of modulatingcompounds.

A potential high throughput method for determining ion channelmodulation utilizes fluorescent dyes that produce a fluorescent signalwhen the cell membrane potential changes. Increases in fluorescenceoccur, because upon a change in the membrane potential, the fluorescentdyes “flip” their orientation in the cell membrane bilayer from anintracellular to extracellular location. This flip causes an increase influorescence that is easily detected and quantified usually using anoptical reader. Optical readouts of ion channel function are favorablefor high throughput screening because they are potentially sensitive,versatile, and amenable to miniaturization and automation. Present dayoptical readers detect fluorescence from multiple samples in a shorttime and can be automated. Fluorescence readouts are used widely both tomonitor intracellular ion concentrations and to measure membranepotentials.

In an attempt to overcome some of the shortcomings of traditionalfluorescent dyes, modified bisoxonol fluorescent dyes such as the FLIPR®Membrane. Potential dyes (FMP) from Molecular Devices were developed.FMP dyes have been effective in correlating fluorescence with membranepotential determined directly by patch-clamp recording for “slow” ionchannels (Baxter et al., J. Biomol. Screen. 7:79-85 (2002); Behrendt etal., British J. Pharmacol. 141:737-745 (2004); and Whiteaker et al., J.Biomol. Screen. 6:305-312 (2001).

A major challenge in designing a high throughput screening (HTS) methodfor compounds that modulate a specific ion channel is that methods ofdetermining channel activation are indirect. To identify compounds thataffect taste through modulation of TRPM5 activity, there must be ademonstration that the effect of the compounds on taste is specific toTRPM5 and not also to one or more of the multitude of other channels andreceptors located on the cell surface. Additionally, since TRPM5activation is calcium dependent, specificity of the TRPM5/test compoundinteraction must be confirmed by excluding those compounds that alsomodulate GPCR-agonist calcium flux.

Therefore, there exists a need in the art for HTS assays that candistinguish compounds that modulate taste by specifically acting onTRPM5, from compounds that may act by other mechanisms and that may notaffect taste perception. The claimed invention provides HTS methods thatgive rapid and specific results, have a high signal to background ratio,and are easy to use.

BRIEF SUMMARY OF THE INVENTION

A new high throughput screening assay has been discovered that allowsfor the rapid screening of compounds that modulate TRPM5 ion channelactivity. The method of the invention is more selective than methodsthat rely only on evaluation of a change in membrane potential. Theinvention will allow a practitioner to distinguish agents that arenonspecific modulators of ion channels from agents that act viamodulation of TRPM5. Moreover, the method will allow thousands ofcompounds that potentially modulate this fast ion channel, and affecttaste, to be screened quickly and reliably.

An embodiment of the present invention is a high throughput screeningassay for screening potential enhancers of the TRPM5 ion channelcomprising contacting a cell expressing TRPM5 with a suboptimalconcentration of an agent that increases intracellular calciumconcentration, wherein the cell has been preloaded with a membranepotential fluorescent dye; contacting said cell with a potentialenhancing compound; using an optical detector, measuring the fluorescentintensity of said cell in the presence of said potential enhancingcompound; and comparing the measured fluorescent intensity to thefluorescent intensity of a different cell expressing TRPM5 in thepresence of an optimal concentration of an agent that increasesintracellular calcium concentration.

An additional embodiment of the invention is a high throughput screeningassay for determining whether a test compound is a TRPM5 ionchannel-specific modulator comprising contacting a cell that expressesTRPM5 and has been preloaded with a membrane potential fluorescent dye,with a test compound in the presence of potassium chloride; using anoptical detector, measuring the fluorescent intensity of said cell inthe presence of said potential modulating compound; comparing themeasured fluorescent intensity determined above to the fluorescentintensity of a different cell that expresses TRPM5 and has beenpreloaded with a membrane potential dye in the presence of potassiumchloride and the absence of the test compound; and evaluating whetherthe test compound may be a TRPM5-specific modulator by determining ifthe ratio of the fluorescent intensity with KCl and the test compound tothe intensity with KCl in the absence of the test compound is less thanor greater than 1.

An additional embodiment of the invention is a high throughput screeningassay for determining whether a test compound is a TRPM5 ionchannel-specific modulator comprising contacting a cell that expressesTRPM5 and has been preloaded with an intracellular calcium dye, with atest compound and a suboptimal concentration of a calcium modulatingagent that increases intracellular calcium concentration; using anoptical detector, measuring the fluorescent intensity of said cell inthe presence of said calcium modulating compound; comparing the measuredfluorescent intensity determined above to the fluorescent intensity of adifferent cell that expresses TRPM5 and has been preloaded with anintracellular calcium dye, in the presence of a suboptimal concentrationof a calcium modulating agent and the absence of the test compound; andevaluating whether the test compound may be a TRPM5-specific modulatorby determining if the ratio of the fluorescent intensity with asuboptimal concentration of a calcium modulating agent and the testcompound, to the intensity with a suboptimal concentration of a calciummodulating agent in the absence of the test compound is less than orgreater than 1.

Another embodiment of the claimed invention is a high throughputscreening assay for screening potential enhancers of the TRPM5 ionchannel comprising contacting a cell expressing both wildtype TRPM5 anda nonfunctional TRPM5 and has been preloaded with a membrane potentialfluorescent dye, with a potential enhancer in the presence of an agentthat increases the calcium concentration in said cell; using an opticaldetector, measuring the fluorescent intensity of said cell in thepresence of said potential enhancer; and comparing the measuredfluorescent intensity determined above to the fluorescent intensity of acell that expresses wildtype TRPM5 and that has been preloaded with amembrane potential dye, in the presence of the potential enhancingcompound to determine the extent of TRPM5 enhancement.

In some embodiments, the nonfunctional TRPM5 contains a deletion of thefirst 1000 base pairs of the TRPM5 gene. In another embodiment, thenonfunctional TRPM5 contains a deletion of the first 2000 base pairs ofthe TRPM5 gene.

In some embodiments, the claimed method further comprises selecting acompound that enhances TRPM5 activity. In other embodiments, the claimedmethod further comprises selecting a compound that inhibits TRPM5activity.

In additional embodiments, the claimed method is directed to screeningcells that are located in a multi-well vessel. The multi-well vessels ofthe claimed invention may contain up to and a number equaling 96 wells.In another embodiment, the multi-well vessel comprises greater than 96wells. In another embodiment, the multi-well vessel comprises 384 wells.In yet another embodiment, the multi-well vessel comprises 1536 wells.

In some embodiments of the claimed invention, agents that increasecalcium concentration are selected from the group consisting ofthrombin, adenosine triphosphate (ATP), carbachol, and agonists ofendogenous G protein coupled receptors (GPCRs). In one embodiment of theinvention, the agent that increases calcium concentration is a calciumionophore, e.g. A23187, calcimycin or ionomycin.

In some embodiments of the claimed invention, the membrane potentialfluorescent dye is a FMP dye.

In additional embodiments of the claimed invention, the optical detectoris selected from the group consisting of: Fluorescent Imaging PlateReader (FLIPR®), FLEXStation, Voltage/Ion Probe Reader (VIPR),fluorescent microscope and charge-coupled device (CCD) camera, andPathway HT. In one embodiment of the invention, the optical detector isa FLIPR®.

Further embodiments, features, and advantages of the present inventions,as well as the structure and operation of the various embodiments of thepresent invention, are described in detail below with reference to theaccompanying drawings.

BRIEF DESCRIPTION OF THE DRAWINGS/FIGURES

The accompanying drawings, which are incorporated herein and form a partof the specification, illustrate one or more embodiments of the presentinvention and, together with the description, further serve to explainthe principles of the invention and to enable a person skilled in thepertinent art to make and use the invention.

FIG. 1 shows a demonstration of TRPM5-dependent fluorescent signaling inChinese Hamster Ovary (CHO) cells. CHO cells transfected with both thehuman TRPM5 ion channel and with the muscarinic 1 (M1) G protein coupledreceptor (GPCR) were loaded with membrane potential dye and stimulatedwith carbachol, an M1 agonist. This GPCR activation triggers an increasein intracellular calcium ions in the cell, which in turn opens the TRPM5ion channel letting primarily sodium ions into the cell. Thisdepolarization increases the fluorescent signal of the dye which ismeasured on the Fluorescent Imaging Plate Reader (FLIPR®). Note that inan assay analyzing the effect of compounds on TRPM5, the compound wouldbe added prior to activation of TRPM5.

FIG. 2 shows TRPM5-GFP expression in transiently-transfected HEK 293cells by fluorescence microscopy.

FIG. 3 shows TRPM5 ion channel responses in transiently transfected HEK293 cells. FIGS. 3A-C show TRPM5 responses in transfected cells inresponse to three GPCR agonists: thrombin (FIG. 3A), carbachol (FIG. 3B)and adenosine triphosphate (ATP) (FIG. 3C) measured using a FLEXstation.

FIG. 4 shows High and Low controls for the TRPM5 high throughputscreening assay using a FLIPR-Tetra™. The assay has a high signal tonoise (High Control vs Low Controls) with a Z′ value of 0.76. A value ofZ′>0.5 indicates a robust assay for high throughput screening. (Zhang,J. H. et al. J. Biomol. Screen. 4:67-73 (1999)).(Z′=1−((3*SD_(HC)+3*SD_(LC))/(AVG_(HC)−AVG_(LC))).

FIGS. 5A-5C show stimulation of cells stably expressing TRPM5 using ATP(FIG. 5A), carbachol (FIG. 5B) or thrombin (FIG. 5C) measured using aFLIPR®.

FIG. 6 shows results from a TRPM5 high throughput screen on greater than85,000 compounds. The data is presented as frequency distribution ofpercent inhibition of control responses. Each compound was tested at aconcentration of 10 μM.

FIG. 7 shows a schematic representation of the TRPM5 specificity filterusing Ca++ response and KCl counterscreen assays.

FIGS. 8A-8B show that KCl counterscreen (FIG. 8A) and Ca++ flux (FIG.8B) filters identify non-selective inhibitory compounds.

FIGS. 9A-9C show the usefulness of the KCl counterscreen in the TRPM5assay to identify TRPM5-specific inhibitors. FIG. 9A demonstrates theidentification of a TRPM5-specific inhibitor measured using a FLIPR®.FIG. 9B shows a dose responsive inhibition of TRPM5 by a compoundwithout inhibiting KCl depolarization or inhibition of calcium fluxactivation. FIG. 9C shows two examples of non-specific inhibition ofTRPM5.

FIG. 10 shows the ability of the KCl counterscreen in the TRPM5 assay toidentify TRPM5-specific enhancer compounds.

FIG. 11 shows the dose responsive stimulation of TRPM5 activity using aTRPM5-specific enhancer (compound 4).

FIG. 12 shows that compound 5 (30 μM) produces a very strong enhancement(17 fold at EC₁₀) of TRPM5 particularly at suboptimal concentrations ofATP.

FIGS. 13A-13B shows the effect of a TRPM5 deletion mutant on the abilityof the calcium ionophore A23187 (FIG. 13A) or carbachol (FIG. 13B) tocause TRPM5-mediated stimulation.

DETAILED DESCRIPTION OF THE INVENTION Overview

The invention is a high throughput screening assay for compounds thatmodulate the activity of TRPM5. Since regulators of TRPM5 are likely toaffect taste sensation, the invention, therefore, provides the firsthigh throughput screening method useful for the identification oftastants that may specifically modulate TRPM5. This method is moreselective than other screens for compounds that may impact taste becausethis method employs counterscreening, the use of suboptimal dosing, anddominant negative mutants of TRPM5.

High throughput refers to processing many compounds in a short timeperiod. For example, using the invention, greater than 1000 testcompounds may be screened for the ability to modulate TRPM5 activity inone hour. This assay is performed using a cell that expresses TRPM5. Asused in the specification and claims, the singular form “a”, “an” and“the” include plural references unless the context clearly dictatesotherwise. For example, the term “an ion channel” includes a pluralityof ion channels. The term “a cell” includes a plurality of cells.

The cell is exposed to a test compound and the ability of that compoundto stimulate opening or to block opening of the channel is measured. Theeffect of the test compound is determined by measuring the change in thecell membrane potential after the cell is exposed to the compound. Afluorescent dye that responds to changes in cell membrane potential isused for detection. A means of evaluating specificity of the ability ofthe compound to modulate the channel is performed in parallel with theabove described method. These parallel methods include the use of apotassium chloride counterscreen, the use of suboptimal doses ofcompounds known to stimulate the channel, and the use of adominant-negative TRPM5 channel that is biologically inactive.

While specific configurations and arrangements are discussed, it shouldbe understood that this is done for illustrative purposes only. A personskilled in the pertinent art will recognize that other configurationsand arrangements can be used without departing from the spirit and scopeof the present invention. It will be apparent to a person skilled in thepertinent art that this invention can also be employed in a variety ofother applications.

Cells

Cells for use in the method of the invention contain either a functionalor non-functional TRPM5. The practitioner may use cells in which TRPM5is endogenous or may introduce TRPM5 into a cell. If TRPM5 is endogenousto the cell, but the level of expression is not optimum, thepractitioner may increase the level of expression of TRPM5 in the cell.Where a given cell does not produce TRPM5 at all, or at sufficientlevels, a TRPM5 nucleic acid may be introduced into a host cell forexpression and insertion into the cell membrane. The introduction, whichmay be generally referred to without limitation as “transformation”, mayemploy any available technique. For eukaryotic cells, suitabletechniques may include calcium phosphate transfection, DEAE-Dextran,electroporation, liposome-mediated transfection and transduction usingretrovirus or other virus, e.g. vaccinia or, for insect cells,baculovirus. General aspects of mammalian cell host systemtransformations have been described in U.S. Pat. No. 4,399,216. Forvarious techniques for transforming mammalian cells, see Keown et al.,Meth. Enzym., 185:527-537 (1990) and Mansour et al., Nature 336:348-352(1988). As is described in detail below, TRPM5 can also be renderednon-functional. Biologically inactive TRPM5 can be introduced into cellsusing any of the above-described techniques. Cells expressing inactiveTRPM5 are useful for confirmation of the specificity of TRPM5activation.

The TRPM5 gene is expressed as a 4.5 kb transcript in a variety of fetaland adult tissues (Prawitt et al. Hum. Mol. Gen. 9:203-216 (2000)).Human TRPM5 has a putative reading frame containing 24 exons whichencode an 1165 amino acid, membrane spanning polypeptide. The NationalCenter for Biotechnology Information (NCBI) database lists severalsequences for both the nucleic acid (NP_(—)064673, NP_(—)055370,AAP44477, AAP44476) and amino acid (NM_(—)014555, NM_(—)020277,AY280364, AY280365) sequences for both the human and mouse forms ofTRPM5, respectively. The inclusion of the above sequences is for thepurpose of illustration of the TRPM5 genetic sequence, however theinvention is not limited to one of the disclosed sequences.

It is recognized in the art that there can be significant heterogeneityin a gene sequence depending on the source of the isolated sequence. Theinvention contemplates the use of conservatively modified variants ofTRPM5. Conservatively modified variants applies to both amino acid andnucleic acid sequences. With respect to particular nucleic acidsequences, conservatively modified variants refers to those nucleicacids which encode identical or essentially identical amino acidsequences, or where the nucleic acid does not encode an amino acidsequence to essentially identical sequences. Because of the degeneracyof the genetic code, a large number of functionally identical nucleicacids encode any given protein.

For instance, the codons GCA, GCC, GCG and GCU all encode the amino acidalanine. Thus, at every position where an alanine is specified by acodon, the codon can be altered to any of the corresponding codonsdescribed without altering the encoded polypeptide. Such nucleic acidvariations are “silent variations,” which are one species ofconservatively modified variations. Every nucleic acid sequence herein,which encodes a polypeptide, also describes every possible silentvariation of the nucleic acid. One of skill will recognize that eachcodon in a nucleic acid (except AUG, which is ordinarily the only codonfor methionine, and TGG, which is ordinarily the only codon fortryptophan) can be modified to yield a functionally identical molecule.Accordingly, each silent variation of a nucleic acid, which encodes apolypeptide, is implicit in each described sequence.

Conservative substitution tables providing functionally similar aminoacids are well known in the art. For example, one exemplary guideline toselect conservative substitutions includes (original residue followed byexemplary substitution): ala/gly or ser; arg/lys; asn/gln or his;asp/glu; cys/ser; gln/asn; gly/asp; gly/ala or pro; his/asn or gln;ile/leu or val; leu/ile or val; lys/arg or gln or glu; met/leu or tyr orile; phe/met or leu or tyr; ser/thr; thr/ser; trp/tyr; tyr/trp or phe;val/ile or leu. An alternative exemplary guideline uses the followingsix groups, each containing amino acids that are conservativesubstitutions for one another: 1) Alanine (A), Serine (S), Threonine(T); 2) Aspartic acid (D), Glutamic acid (E); 3) Asparagine (N),Glutamine (Q); 4) Arginine (R), Lysine (I); 5) Isoleucine (I), Leucine(L), Methionine (M), Valine (V); and 6) Phenylalanine (F), Tyrosine (Y),Tryptophan (W); (see also, e.g., Creighton, Proteins, W. H. Freeman andCompany (1984); Schultz and Schimer, Principles of Protein Structure,Springer-Verlag (1979)). One of skill in the art will appreciate thatthe above-identified substitutions are not the only possibleconservative substitutions. For example, for some purposes, one mayregard all charged amino acids as conservative substitutions for eachother whether they are positive or negative. In addition, individualsubstitutions, deletions or additions that alter, add or delete a singleamino acid or a small percentage of amino acids in an encoded sequencecan also be considered “conservatively modified variations.”

Dominant negative forms of TRPM5 may also be used in the high throughputscreening assay to identify compounds that specifically modulate TRPM5.By “dominant negative” herein is meant a protein comprising at least onevariant TRPM5 monomer that competes for binding to wildtype subunitssuch that the protein retains the ability to form an ion channel but itcannot regulate the flux of monovalent cations. Depending on thecomposition of the ion channel, the degree to which monovalent cationflux is inhibited will vary.

The variant TRPM5 proteins of the invention comprise non-conservativemodifications (e.g. substitutions). By “nonconservative” modificationherein is meant a modification in which the wildtype residue and themutant residue differ significantly in one or more physical properties,including hydrophobicity, charge, size, and shape. For example,modifications from a polar residue to a nonpolar residue or vice-versa,modifications from positively charged residues to negatively chargedresidues or vice versa, and modifications from large residues to smallresidues or vice versa are nonconservative modifications. For example,substitutions may be made which more significantly affect: the structureof the polypeptide backbone in the area of the alteration, for examplethe alpha-helical or beta-sheet structure; the charge or hydrophobicityof the molecule at the target site; or the bulk of the side chain. Thesubstitutions which in general are expected to produce the greatestchanges in the polypeptide's properties are those in which (a) ahydrophilic residue, e.g. seryl or threonyl, is substituted for (or by)a hydrophobic residue, e.g. leucyl, isoleucyl, phenylalanyl, valyl oralanyl; (b) a cysteine or proline is substituted for (or by) any otherresidue; (c) a residue having an electropositive side chain, e.g. lysyl,arginyl, or histidyl, is substituted for (or by) an electronegativeresidue, e.g. glutamyl or aspartyl; or (d) a residue having a bulky sidechain, e.g. phenylalanine, is substituted for (or by) one not having aside chain, e.g. glycine. In one embodiment, the variant TRPM5 proteinsof the present invention have at least one nonconservative modification.In one embodiment, the variant TRPM5 protein results from translation ofa polynucleotide in which the first 1000 base pairs of the TRPM5 genehave been deleted. In another embodiment, the variant TRPM5 proteinresults from translation of a polynucleotide in which the first 2000base pairs of the TRPM5 gene have been deleted.

The variant proteins may be generated, for example, by using a PDA™system previously described in U.S. Pat. Nos. 6,188,965; 6,296,312;6,403,312; alanine scanning (see U.S. Pat. No. 5,506,107), geneshuffling (WO 01/25277), site saturation mutagenesis, mean field,sequence homology, polymerase chain reaction (PCR) or other methodsknown to those of skill in the art that guide the selection of point ordeletion mutation sites and types.

The cells used in methods of the present invention may be present in, orextracted from, organisms, may be cells or cell lines transiently orpermanently transfected or transformed with the appropriate proteins ornucleic acids encoding them, or may be cells or cell lines that expressthe required TRPM5 from endogenous (i.e. not artificially introduced)genes.

Expression of the TRPM5 protein refers to the translation of the TRPM5polypeptide from a TRPM5 gene sequence either from an endogenous gene orfrom nucleic acid introduced into a cell. The term “in situ” where usedherein includes all these possibilities. Thus in situ methods may beperformed in a suitably responsive cell line which expresses the TRPM5(either as a native channel, or from a nucleic acid introduced into thecell). The cell line may be in tissue culture or may be, for example, acell line xenograft in a non-human animal subject.

As used herein, the term “cell membrane” refers to a lipid bilayersurrounding a biological compartment, and encompasses an entire cellcomprising such a membrane, or a portion of a cell.

For stable transfection of mammalian cells, depending upon theexpression vector and transfection technique used, only a small fractionof cells may integrate the foreign DNA into their genome. In order toidentify and select these integrants, a gene that encodes a selectablemarker (e.g., resistance to antibiotics) is generally introduced intothe host cell along with the gene of interest. Preferred selectablemarkers include those which confer resistance to drugs, such as G418,hygromycin and methotrexate. A nucleic acid encoding a selectable markercan be introduced into a host cell in the same vector as that encodingTRPM5, or can be introduced in a separate vector. Cells stablytransfected with the introduced nucleic acid can be identified by drugselection (e.g., cells that have incorporated the selectable marker genewill survive, while the other cells die).

It should be noted that expression of TRPM5 can also be controlled byany of a number of inducible promoters known in the art, such as atetracycline responsive element, TRE. For example, TRPM5 can beselectively presented on the cell membrane by controlled expressionusing the Tet-on and Tet-off expression systems provided by Clontech(Gossen, M. and Bujard, H. Proc. Natl. Acad. Sci. USA 89: 5547-5551(1992)). In the Tet-on system, gene expression is activated by theaddition of a tetracycline derivative doxycycline (Dox), whereas in theTet-off system, gene expression is turned on by the withdrawal oftetracyline (Tc) or Dox. Any other inducible mammalian gene expressionsystem may also be used. Examples include systems using heat shockfactors, steroid hormones, heavy metal ions, phorbol ester andinterferons to conditionally expressing genes in mammalian cells.

The cell lines used in assays of the invention may be used to achievetransient expression of TRPM5, or may be stably transfected withconstructs that express a TRPM5 peptide. Means to generate stablytransformed cell lines are well known in the art and such means may beused here. Examples of cells include, but are not limited to ChineseHamster Ovary (CHO) cells, COS-7, HeLa, HEK 293, PC-12, and BAF.

The level of TRPM5 expression in a cell may be increased by introducinga TRPM5 nucleic acid into the cells or by causing or allowing expressionfrom a heterologous nucleic acid encoding TRPM5. A cell may be used thatendogenously expresses TRPM5 without the introduction of heterologousgenes. Such a cell may endogenously express sufficient levels of TRPM5for use in the methods of the invention, or may express only low levelsof TRPM5 which require supplementation as described herein.

The level of TRPM5 expression in a cell may also be increased byincreasing the levels of expression of the endogenous gene. Endogenousgene activation techniques are known in the art and include, but are notlimited to, the use of viral promoters (WO 93/09222; WO 94/12650 and WO95/31560) and artificial transcription factors (Park et al. Nat.Biotech. 21:1208-1214 (2003).

The level of TRPM5 expression in a cell may be determined by techniquesknown in the art, including but not limited to, nucleic acidhybridization, polymerase chain reaction, RNase protection, dotblotting, immunocytochemistry and Western blotting. Alternatively, TRPM5expression can be measured using a reporter gene system. Such systems,which include for example red or green fluorescent protein (see, e.g.Mistili and Spector, Nature Biotechnology 15:961-964 (1997), allowvisualization of the reporter gene using standard techniques known tothose of skill in the art, for example, fluorescence microscopy.Furthermore, the ability of TRPM5 to be activated by known positivemodulating compounds, such as thrombin, may be determined followingmanipulation of the TRPM5 expressing cells.

Cells described herein may be cultured in any conventional nutrientmedia. The culture conditions, such as media, temperature, pH and thelike, can be selected by the skilled artisan without undueexperimentation. In general, principles, protocols, and practicaltechniques for maximizing the productivity of cell cultures can be foundin “Mammalian Cell Biotechnology: a Practical Approach”, M. Butler, ed.JRL Press, (1991) and Sambrook et al, supra.

Intracellular Calcium Activation

TRPM5 is a calcium-activated ion channel permeable to monovalent cationssuch as sodium. Therefore, in order to observe channel activity, calciumstores within the cells must first be activated. There are many methodsto activate intracellular calcium stores and many calcium activatingagents are known in the art and include, but are not limited tothrombin, adenosine triphosphate (ATP), carbachol, and calciumionophores (e.g. A23187). While nanomolar increases in calciumconcentration ranges are required for TRPM5 channel activation, theconcentration ranges useful for the claimed invention are known in theart, e.g., between 10⁻¹⁰ to 10⁻⁴ M for ATP, however, the preciseconcentration may vary depending on a variety of factors including celltype and time of incubation. The increased calcium concentration can beconfirmed using calcium sensitive dyes, e.g., Fluo 3, Fluo 4, or FLIPRcalcium. 3 dye and single cell imaging techniques in conjunction withFura2.

As described below, application of suboptimal doses of calciumactivating agents can be used as a secondary screen for TRPM5 modulatingspecificity. Test cells are incubated with lower doses of the calciumactivating agents described above, such that a fluorescent response thatis lower than the maximum achievable response is generated. Generally,the dose is referred to as the effect concentration or EC₂₀₋₃₀, whichrelates to the effect condition where the fluorescent intensity is20-30% of the maximal response. As used herein, “EC” refers to effectcondition, such that EC₂₀ refers to the effect condition where thefluorescent intensity is 20% of the maximal response is generated. Uponthe addition of a TRPM5-specific activating compound, this low responsewill be increased to at, or near, maximal levels of activation.

Counterscreening techniques are also useful for identifyingTRPM5-specific modulating compounds. The ability to distinguishcompounds specific for TRPM5 inhibition and activation from compoundsthat modulate other ion channels, in addition to, or instead of TRPM5,particularly channels not involved in taste transduction is vital. Asdescribed in greater detail below, potassium chloride non-specificallyactivates a number of ion channels, but not TRPM5. Therefore, KClactivation can be used as a counterscreen to identify TRPM5-specificmodulating compounds.

Fluorescent Dyes

Voltage sensitive dyes that may be used in the assays and methods of theinvention have been used to address cellular membrane potentials(Zochowski et al., Biol. Bull. 198:1-21 (2000)). Membrane potential dyesor voltage-sensitive dyes refer to molecules or combinations ofmolecules that enter depolarized cells, bind to intracellular proteinsor membranes and exhibit enhanced fluorescence. These dyes can be usedto detect changes in the activity of an ion channel such as TRPM5,expressed in a cell. Voltage-sensitive dyes include, but are not limitedto, modified bisoxonol dyes, sodium dyes, potassium dyes and thoriumdyes. The dyes enter cells and bind to intracellular proteins ormembranes, therein exhibiting enhanced fluorescence and red spectralshifts (Epps et al., Chem. Phys. Lipids 69:137-150 (1994)). Increaseddepolarization results in more influx of the anionic dye and thus anincrease in fluorescence.

The TRPM5 cells of the assay are preloaded with the membrane potentialdyes for 30-240 minutes prior to addition of test compounds. Preloadingrefers to the addition of the fluorescent dye for a period prior to testcompound addition during which the dye enters the cell and binds tointracellular lipophilic moieties.

In one embodiment, the membrane potential dyes are FMP dyes availablefrom Molecular Devices (Catalog Nos. R8034, R8123). In otherembodiments, suitable dyes could include dual wavelength FRET-based dyessuch as DiSBAC2, DiSBAC3, and CC-2-DMPE (Invitrogen Cat. No. K1016).[Chemical Name Pacific Blue™1,2-ditetradecanoyl-sn-glycero-3-phosphoethanolamine, triethylammoniumsalt]. Cells are typically treated with 1 to 10 μM buffered solutions ofthe dye for 20 to 60 minutes at 37° C.

Dyes that measure intracellular calcium levels are also used to confirmTRPM5 specificity. In one embodiment, the intracellular calcium dye isthe FLIPR Calcium 3 dye available from Molecular Devices (Part Number:R8091). In other embodiments, suitable dyes such as Fluo-3, Fluo-4(Invitrogen (Cat. Numbers F14242 and F14202) can be used to measureincreases in intercellular calcium. Cells are typically treated with 1to 10 μM buffered solutions of the dye for 20 to 60 minutes at 37° C. Insome cases it is necessary to remove the dye solutions from the cellsand add fresh assay buffer before proceeding with the assay.

Assay Detection

Detecting and recording alterations in the spectral characteristics ofthe dye in response to changes in membrane potential may be performed byany means known to those skilled in the art. As used herein, a“recording” refers to collecting and/or storing data obtained fromprocessed fluorescent signals, such as are obtained in fluorescentimaging analysis.

In some embodiments, the assays of the present invention are performedon isolated cells using microscopic imaging to detect changes inspectral (i.e., fluorescent) properties. In other embodiments, the assayis performed in a multi-well format and spectral characteristics aredetermined using a microplate reader.

By “well” it is meant generally a bounded area within a container, whichmay be either discrete (e.g., to provide for an isolated sample) or incommunication with one or more other bounded areas (e.g., to provide forfluid communication between one or more samples in a well). For example,cells grown on a substrate are normally contained within a well that mayalso contain culture medium for living cells. Substrates can compriseany suitable material, such as plastic, glass, and the like. Plastic isconventionally used for maintenance and/or growth of cells in vitro.

A “multi-well vessel”, as noted above, is an example of a substratecomprising more than one well in an array. Multi-well vessels useful inthe invention can be of any of a variety of standard formats (e.g.,plates having 2, 4, 6, 24, 96, 384, or 1536, etc., wells), but can alsobe in a non-standard format (e.g., plates having 3, 5, 7, etc., wells).

A suitable configuration for single cell imaging involves the use of amicroscope equipped with a computer system. One example of such aconfiguration, ATTO's Attofluor® RatioVision® real-time digitalfluorescence analyzer from Carl Zeiss, is a completely integrated workstation for the analysis of fluorescent probes in living cells andprepared specimens (ATTO, Rockville, Md.). The system can observe ionseither individually or simultaneously in combinations limited only bythe optical properties of the probes in use. The standard imaging systemis capable of performing multiple dye experiments such as FMP (forsodium) combined with GFP (for transfection) in the same cells over thesame period of time. Ratio images and graphical data from multiple dyesare displayed online.

When the assays of the invention are performed in a multi-well format, asuitable device for detecting changes in spectral qualities of the dyesused is a multi-well microplate reader. Suitable devices arecommercially available, for example, from Molecular Devices(FLEXstation® microplate reader and fluid transfer system or FLIPR®system), from Hamamatsu (FDSS 6000) and the “VIPR” voltage ion probereader (Aurora, Bioscience Corp. CA, USA). The FLIPR-Tetra™ is a secondgeneration reader that provides real-time kinetic cell-based assaysusing up to 1536 simultaneous liquid transfer systems. All of thesesystems can be used with commercially available dyes such as FMP, whichexcites in the visible wavelength range.

Using the FLIPR® system, the change in fluorescent intensity ismonitored over time and is graphically displayed as shown, for examplein FIGS. 9A-9C. The addition of TRPM5 enhancing compounds causes anincrease in fluorescence, while TRPM5 blocking compounds block thisincrease.

Several commercial fluorescence detectors are available that can injectliquid into a single well or simultaneously into multiple wells. Theseinclude, but are not limited to, the Molecular Devices FlexStation(eight wells), BMG NovoStar (two wells) and Aurora VIPR (eight wells).Typically, these instruments require 12 to 96 minutes to read a 96-wellplate in flash luminescence or fluorescence mode (1 min/well). Analternative method is to inject the modulator into all sample wells atthe same time and measure the luminescence in the whole plate by imagingwith a charge-coupled device (CCD) camera, similar to the way thatcalcium responses are read by calcium-sensitive fluorescent dyes in theFLIPR®, FLIPR-384 or FLIPR-Tetra™ instruments. Other fluorescenceimaging systems with integrated liquid handling are expected from othercommercial suppliers such as the second generation LEADSEEKER fromAmersham, the Perkin Elmer CellLux-Cellular Fluorescence Workstation andthe Hamamatsu FDSS6000 System. These instruments can generally beconfigured to proper excitation and emission settings to read FMP dye(540_(ex)±15 nm, 570_(em)±15 nm) and calcium dye (490_(ex)±15 nm,530_(em)±15 nm). The excitation/emission characteristics differ for eachdye, therefore, the instruments are configured to detect the dye chosenfor each assay.

Test Compounds

Test compounds employed in the screening methods of this inventioninclude for example, without limitation, synthetic organic compounds,chemical compounds, naturally occurring products, polypeptides andpeptides, nucleic acids, etc.

Essentially any chemical compound can be used as a potential modulatoror ligand in the assays of the invention. Most often compounds dissolvedin aqueous or organic (especially dimethyl sulfoxide- or DMSO-based)solutions are used. The assays are designed to screen large chemicallibraries by automating the assay steps. The compounds are provided fromany convenient source to the cells. The assays are typically run inparallel (e.g., in microtiter formats on microtiter plates in roboticassays with different test compounds in different wells on the sameplate). It will be appreciated that there are many suppliers of chemicalcompounds, including ChemDiv (San Diego, Calif.), Sigma-Aldrich (St.Louis, Mo.), Fluka Chemika-Biochemica-Analytika (Buchs Switzerland) andthe like.

“Modulating” as used herein includes any effect on the functionalactivity of TRPM5. This includes blocking or inhibiting the activity ofthe channel in the presence of, or in response to, an appropriatestimulator. Alternatively, modulators may enhance the activity of thechannel. “Enhance” as used herein, includes any increase in thefunctional activity of TRPM5.

In one embodiment, the high throughput screening methods involveproviding a small organic molecule or peptide library containing a largenumber of potential TRPM5 modulators. Such “chemical libraries” are thenscreened in one or more assays, as described herein, to identify thoselibrary members (particular chemical species or subclasses) that displaya desired characteristic activity. The compounds thus identified canserve as conventional “lead compounds” or can themselves be used aspotential or actual products.

A combinatorial chemical library is a collection of diverse chemicalcompounds generated by either chemical synthesis or biologicalsynthesis, by combining a number of chemical “building blocks” such asreagents. For example, a linear combinatorial chemical library such as apolypeptide library is formed by combining a set of chemical buildingblocks (amino acids) in every possible way for a given compound length(i.e., the number of amino acids in a polypeptide compound). Millions ofchemical compounds can be synthesized through such combinatorial mixingof chemical building blocks.

Preparation and screening of combinatorial chemical libraries is wellknown to those of skill in the art. Such combinatorial chemicallibraries include, but are not limited to, peptide libraries (see, e.g.,U.S. Pat. No. 5,010,175; Furka Int. J. Pept. Prot. Res. 37:487-493(1991) and Houghton et al., Nature 354:84-88 (1991)). Other chemistriesfor generating chemical diversity libraries can also be used. Suchchemistries include, but are not limited to: peptoids (e.g., PCTPublication No. WO 91/19735), encoded peptides (e.g., PCT PublicationNo. WO 93/20242), random bio-oligomers (e.g., PCT Publication No. WO92/00091), benzodiazepines (e.g., U.S. Pat. No. 5,288,514), diversomerssuch as hydantoins, benzodiazepines and dipeptides (Hobbs et al., Proc.Nat. Acad. Sci. USA 90:6909-6913 (1993)), vinylogous polypeptides(Hagihara et al., J. Amer. Chem. Soc. 114:6568 (1992)), nonpeptidalpeptidomimetics with glucose scaffolding (Hirschmann et al., J. Amer.Chem. Soc. 114:9217-9218 (1992)), analogous organic syntheses of smallcompound libraries (Chen et al., J. Amer. Chem. Soc. 116:2661 (1994)),oligocarbamates (Cho et al., Science 261:1303 (1993)), and/or peptidylphosphonates (Campbell et al., J. Org. Chem. 59:658 (1994)), nucleicacid libraries (see Ausubel, Berger and Sambrook, all supra), peptidenucleic acid libraries (see, e.g., U.S. Pat. No. 5,539,083), antibodylibraries (see, e.g., Vaughn et al., Nature Biotechnology, 14:309-314(1996) and PCT/US96/10287), carbohydrate libraries (see, e.g., Liang etal., Science, 274:1520-1522 (1996) and U.S. Pat. No. 5,593,853), smallorganic molecule libraries (see, e.g., isoprenoids, U.S. Pat. No.5,569,588; thiazolidinones and metathiazanones, U.S. Pat. No. 5,549,974;pyrrolidines, U.S. Pat. Nos. 5,525,735 and 5,519,134; morpholinocompounds, U.S. Pat. No. 5,506,337; benzodiazepines, U.S. Pat. No.5,288,514, and the like).

Devices for the preparation of combinatorial libraries are commerciallyavailable (see, e.g., 357 MPS, 390 MPS, Advanced Chem Tech, LouisvilleKy.; Symphony, Rainin, Woburn, Mass.; 433A Applied Biosystems, FosterCity, Calif.; 9050 Plus, Millipore, Bedford, Mass.). In addition,numerous combinatorial libraries are themselves commercially available(see, e.g., ComGenex, Princeton, N.J.; Asinex, Moscow, Russia; Tripos,Inc., St. Louis, Mo.; ChemStar, Ltd, Moscow, Russia; 3D Pharmaceuticals,Exton, Pa.; Martek Biosciences, Columbia, Md.; etc.).

Candidate agents, compounds, drugs, and the like encompass numerouschemical classes, though typically they are organic molecules,preferably small organic compounds having a molecular weight of morethan 100 and less than about 10,000 daltons, preferably, less than about2000 to 5000 daltons. Candidate compounds may comprise functional groupsnecessary for structural interaction with proteins, particularlyhydrogen bonding, and typically include at least an amine, carbonyl,hydroxyl or carboxyl group, preferably at least two of the functionalchemical groups. The candidate compounds may comprise cyclical carbon orheterocyclic structures, and/or aromatic or polyaromatic structuressubstituted with one or more of the above functional groups. Candidatecompounds are also found among biomolecules including peptides,saccharides, fatty acids, steroids, purines, pyrimidines, derivatives,structural analogs or combinations thereof.

A variety of other reagents may be included in the screening assayaccording to the present invention. Such reagents include, but are notlimited to, salts, solvents, neutral proteins, e.g. albumin, detergents,etc., which may be used to facilitate optimal protein-protein bindingand/or to reduce non-specific or background interactions. Examples ofsolvents include, but are not limited to, dimethyl sulfoxide (DMSO),ethanol and acetone, and are generally used at a concentration of lessthan or equal to 1% (v/v) of the total assay volume. In addition,reagents that otherwise improve the efficiency of the assay, such asprotease inhibitors, anti-microbial agents, etc. may be used. Further,the mixture of components in the method may be added in any order thatprovides for the requisite binding.

The compounds identified using the disclosed assay are potentiallyuseful as ingredients or flavorants in ingestible compositions, i.e.,foods and beverages as wells as orally administered medicinals.Compounds that modulate taste perception can be used alone or incombination as flavorants in foods or beverages. The amount of suchcompound(s) will be an amount that yields the desired degree ofmodulated taste perception of which starting concentrations maygenerally be between 0.1 and 1000 μM.

EXAMPLES Example 1 Imaging-Based High Throughput Screening Assay UsingTransiently-Transfected Cells

As described in greater detail below, HEK 293 cells, transientlytransfected with a plasmid bearing the human TRPM5 gene, were used todevelop the high throughput screening assay. Indirect measurement of thechanges in Na⁺ ions within the HEK 293 cells were made using a FMP dyeand stimulation of the cells using calcium activating agents.

Plasmid Construction

First strand cDNA was synthesized by Thermoscript RT-PCR System(Invitrogen) from human small intestine poly A+ RNA (BD Biosciences) andthe full length hTRPM5 was amplified by PCR using GC Melt (BDBiosciences). The product was PCR purified by Pure Link PCR Purification(Invitrogen) and inserted into a vector using the TOPO TA Cloning Kit(Invitrogen). After sequencing, 6 mutations were found and the mutationswere corrected using the Quick Change Multi Site Directed MutagenesisKit (Stratagene) in 2 rounds. Three mutations were corrected in eachround. The full length TRPM5 was excised from the TOPO TA vector usingthe EcoRI and NotI restriction enzymes and ligated in the pENTR 3Cvector, which had also been digested with EcoRI and NotI. The insert andvector bands were gel extracted and purified using the SNAP GelPurification Kit (Invitrogen). Finally, LR Recombination Reaction(Invitrogen) was used to insert the entry clone into destination vectorsof interest (e.g., pT-Rex-DEST 30, pcDNA-DEST 53, pcDNA 3.2/v5-DEST andpcDNA 6.2/V5-DEST).

Transfection

1.0×10⁶ HEK 293 cells (ATCC) were plated in each well of a 6-well tissueculture dish overnight. The following day, cells were transfected with 4μg of a pcDNA3.2 vector containing TRPM5 cDNA and 8 μl of Lipofectamine2000 (Invitrogen), according to the manufacturer's protocol, andincubated overnight. The following day, transfected cells weretrypsinized and seeded into 96-well black, clear bottom, poly-D-lysineplates (Corning) at a density of 70,000 cells/well in a 100 μl volumeand incubated in a 37° C./5% CO₂ incubator overnight.

Fluorescence Microscopy

To confirm that the HEK transfected cells expressed TRPM5, cellstransiently-transfected with 6 μg of plasmid DNA expressing TRPM5 (asdescribed above) and grown on Lab TekII Chamber slides, were evaluated.Control, untransfected cells were grown in parallel with the transfectedcells. The fluorescent emission of the GFP-TRPM5 expressing cells wasdetected using the green detection channel (515-530 nm) of a fluorescentmicroscope.

Membrane Potential Assay

Once the expression of TRPM5 was confirmed in the HEK cells, 100 μl ofthe Blue or Red FMP dye (Molecular Devices) was added to, each well ofplates seeded with the transiently transfected cells. The plate was thenincubated in a 37° C./5% CO₂ incubator for 1 hour. The plate was read ina FLEXStation microplate reader (Molecular Devices) with an excitationof 530 nm and an emission of 565 nm. The fluorescence was monitored for3 minutes upon exposure of the cells to a calcium activating agent(carbachol, thrombin peptide or ATP).

Results

The TRPM5 plasmid was readily expressed as demonstrated by theappearance of bright green HEK 293 cells that were transfected with theGFP-TRPM5 plasmid (FIG. 2).

Demonstration of TRPM5 response to stimuli is shown in FIG. 3A-3C. TRPM5transfected cells were loaded with FMP dye and then treated withthrombin (FIG. 3A), carbachol (FIG. 3B), or ATP (FIG. 3C) and monitoredfor an increase in cellular fluorescence in the FLEXstation. All threeagents generated a strong spike in relative fluorescence within thefirst 30 seconds of agonist addition. The response was transient innature as well, as fluorescence levels returned to near baseline levelsby approximately 1 minute post-agonist addition. Mock treated cellsproduced a low response in both the ATP and carbachol treated cells,however a high degree of background fluorescence was observed in thethrombin treated group. The fluorescence of the thrombin treated cellswas greater than 4-fold over background, therefore the backgroundfluorescence did not interfere with data interpretation.

The applicability of the screening method of the invention to a highthroughput format is demonstrated in FIG. 4, where samples in a 384-wellplate were evaluated in a 5 minute assay on the FLIPR-Tetra™ (MolecularDevices). TRPM5-Transfected HEK cells, 15,000/well, were seededovernight on poly-D-lysine coated 384 well plates in 20 μl media.Membrane potential dye, 20 μl/well, was added and the plates incubatedfor 1 hour at 37° C. Plates were placed in a FLIPR-Tetra™ andfluorescence readings were taken using appropriate filters. After 10seconds, 10 μl of either buffer or a deactivating agent (ATP) were addedto the cells (first addition). At 200 seconds a second addition of 10 μlof ATP was added to all cells. A strong, reproducible TRP M5 responsewas seen in those cells that received buffer (High Control), while thosethat were initially stimulated with ATP became deactivated and failed torespond to a second addition of ATP (Low Control). There was a >5 folddifference in peak heights (maximum-minimum values over each peak)between the High and Low controls, demonstrating that the assay issuitable for high throughput screening. Furthermore a calculation of Z′*gave a value of 0.76, greater than the HTS acceptable value of 0.5.(Z′=1−((3*SDhigh control+3*SD low control)/(High Control−Low Control)).

Example 2 Imaging-Based High Throughput Screening Assay UsingStably-Transfected Cells

Stimulation of TRPM5 was also visible in HEK cells stably-expressingTRPM5. Following confirmation of TRPM5 expression, the ability toregulate TRPM5 activity was analyzed as described above.

Plasmid Construction and Transfection

HEK cells stably-expressing TRPM5 were generated using the pcDNA 3.2vector containing hTRPM5 using the technique described above. Stableclones were generated by transfecting 1.0×10⁶ HEK 293 cells with 4 μg ofpcDNA 3.2-TrpM5 in a 35 mm tissue culture dish. Two dayspost-transfection, the cells were trypsinized and diluted 1:10 and 1:100in growth medium containing 1 mg/ml Geneticin (Invitrogen) to select forsingle clones. Cells were maintained in this medium until singleindividual clones could be isolated and expanded. Upon selection ofindividual clones, cells were maintained in medium containing 0.25 mg/mlGeneticin to maintain the selective pressure. Individual clones werethen examined with membrane potential dye in the FLEXstation or FLIPR®as described above. Those clones with the largest fluorescent responseto ATP and carbachol were then selected and examined for furtheranalysis. Selected clones with the highest EC₅₀ to ATP and carbacholwere then expanded and used for the high throughput screening assays.

Results

TRPM5 stably expressed in HEK cells was analyzed for its ability torespond to different concentrations of several GPCR agonists. The assaywas performed on a FLIPR® using the excitation 510-545 nm and emission565-625 nm filter sets. Assay plates containing stably expressing HEKcells were loaded with 1× Membrane Potential Assay Dye Red (MolecularDevices) for one hour in a 37° C. and 5% CO₂ incubator. The plates werethen removed from the incubator and equilibrated to room temperature for15 minutes before reading on the FLIPR®. The plates were read on theFLIPR® for a total of 3 minutes. Baseline fluorescence was obtained onthe FLIPR® for 10 seconds followed by addition of each agonist by theFLIPR® and read for an additional 2 minutes and 50 seconds. FIG. 5 showsthat two TRPM5-expressing clones were stimulated by varyingconcentrations of the GPCR agonists as evidenced by an increase in therelative fluorescence of TRPM5-expressing cells compared to shamtransfected cells. The values on the graph represent the difference inthe maximum minus the minimum fluorescence upon agonist addition.Individual clones are represented by clone number, while the pool ofclones represents the sum of all cells that were resistant to selection.In all cases, clone 1 gave the strongest response to all 3 agonists(ATP, carbachol, and thrombin peptide, FIGS. 5A-5C, respectively). Clone5 and pooled clones generated a lower response in comparison to clone 1.However, both the clone 5 and pool responses were a minimum 3-foldhigher than fluorescence in non-transfected cells. Sham, non-transfectedcells showed little or no response at any agonist concentration.

Example 3 High Throughput Screening Assay Using SuboptimalConcentrations of Calcium-Activating Agents

Specificity of potential activating compounds may be identified usingsuboptimal concentrations of agents that increase intracellular calciumlevels. In this type of assay, rather than using a high concentrationof, for example carbachol, a reduced concentration is added toTRPM5-expressing cells with or without an additional test compound.Enhancers of TRPM5 activity are those test compounds that increase thefluorescent intensity in reduced carbachol treated cells, to the levelseen in cells treated to a high dose.

A carbachol dose response curve was generated for the TRPM5 expressingcells so that the suboptimal concentration range could be determined.Cells expressing TRPM5 were incubated with an EC₂₀-EC₃₀ level ofcarbachol (0.3 to 1 μM) prior to addition of test compounds. Mockincubated and EC₁₀₀ treated cells were used as controls. Test compoundsthat increased the fluorescent intensity of EC₂₀-EC₃₀ treated cells tolevels approaching EC₁₀₀ treated cells were classified as activators ofTRPM5.

Example 4 KC₁-Counterscreen for TRPM5 Specificity

The need for enhanced specificity assays for TRPM5 activation is shownin FIG. 6. Greater than 85,000 compounds were screened using theabove-described high throughput screening assays and the Gaussiandistribution of inhibition values was plotted. As is visible in thefigure, most of the compounds were within the −25 to +25 percent rangeof inhibition of the control response. Therefore, in order to identifyTRPM5 modulating compounds with greater specificity, compounds that alsoact on other ion channels would have to be removed from the analysis.

KCl activates a number of ion channels, but not TRPM5. Therefore, KClcan be used as a counterscreen to identify modulating compounds specificfor TRPM5.

The ideal blocker would block TRPM5 but not other channels. The TRPM5assay is conducted as described in Example 3, utilizing a membranepotential dye. A test compound is added, and the cells are thenstimulated with ATP to trigger the channel, leading to a dye response.The process is shown schematically in FIG. 7. The KCl counterscreen isperformed as described in Example 3, with identical cells, pretreatedwith the same compound, but the stimulus was 20 mM KCl, not ATP. KClstimulated and unstimulated responses are used as controls. An exampleof a non-selective inhibitory compound as identified using the KClcounterscreen is shown in FIG. 8A. Compound F001344, A3 (structure shownbelow) inhibits TRPM5, but also the KCl responses (arrows). Anadditional specificity assay utilizes a Ca++ flux dye (Calcium 3 Dye,Part No. R8091) to determine whether or not the compound interferes withagonist-induced Ca++ flux response. An example of a non-selectiveinhibitory compound as identified by the Ca++ flux assay is shown inFIG. 8B. Compound F0013488, C13 (structure shown below) inhibits TRPM5,but also activates the Ca++ flux response (arrows).

FIG. 9A shows FLIPR traces in a TRPM5 assay for 4 concentrations of atest compound, compound 1 (structure shown below). Panel 1 shows doseresponsive inhibition of the TRPM5 response. Panels 2 and 3 demonstratethat increasing dose of the compound does not alter KCl or Ca++responses. The quantitation of the these results is shown in FIG. 9B.Examples of two additional test compounds (compounds 2 and 3) are shownin FIG. 9C, which shows non-specific inhibition TPRM5, where compound 2also inhibits the KCl response and compound 3 inhibits the Ca++response.

The KCl counterscreen is also useful for the identification of selectiveTRPM5 enhancing compounds. FIG. 10 shows the selective enhancement ofTRPM5. The counterscreen experiments were performed as described abovein the presence of test compound 4. TRPM5 expressing HEK and CHO cellsdemonstrated a 131% and 135% maximal stimulation upon addition of testcompound 4, respectively. Addition of increasing amounts of testcompound 4 also resulted in a dose-dependent increase in TRPM5 activity(FIG. 11). Furthermore, very strong enhancement is seen at suboptimal(EC₁₀) concentrations of ATP agonist using compound 5 (FIG. 12).

Example 5 High Throughput Assay Using a Dominant Negative TRPM5

Deletion mutants were generated to examine whether specificity for TRPM5could be achieved using a dominant negative form of the channel. TheN1000 deletion mutant is a form of mTRPM5 in which the first 1000 basepairs of the gene have been deleted and the N2000 deletion mutantcontains a deletion of the first 2000 base pairs of the gene. The first2000 base pairs of the gene correspond to the amino-terminal domain ofthe mTRPM5 ion channel. Deletion of this region results in a truncatedversion of the protein where the entire amino-terminal domain is removedand the protein begins with the first transmembrane region of the ionchannel. The deletion mutants were constructed by PCR using primersdesigned to amplify the gene with the first 1000 base pairs deleted andthe first 2000 base pairs deleted, respectively. The experimentsdescribed below were performed as previously described in terms ofnumber of cells used, incubation times and dyes.

Experiments were performed by comparing transfection of different ratiosof the deletion mutants to wildtype mTRPM5 as compared to the wildtypemTRPM5 with a null vector. The total amount of transfected DNA was keptconstant at 4 μg. 1×10⁶ HEK 293 cells were plated in 6 well dishesovernight. Ratios of deletion mutant mTRPM5/wildtype mTRPM5 and wildtypemTRPM5/pSV3-neo were then transfected into the HEK 293 cells usingLipofectamine 2000 as indicated in Table 1. One day followingtransfection, 15,000 cells/well were plated on 384 plates and maintainedin an incubator overnight. The following day the cells were loaded withmembrane potential dye at 37° C. and response to A23187 and carbacholdose responses were compared.

TABLE 1 Transfections in HEK 293 Cells Followed by TRPM5 AssayExperimental Design Wt-mTrpM5 3.8 μg 3 μg 2 μg 1 μg 0.2 μg 4 μg N10000.2 μg 1 μg 2 μg 3 μg 3.8 μg 0 μg pSV3-neo 0.2 μg 1 μg 2 μg 3 μg 3.8 μg0 μg

As shown in FIGS. 13A-13B, as the concentration of the deletion mutantincreases, the relative fluorescence in response to A23187 (FIG. 13A) orcarbachol (FIG. 13B) decreases. However, the decrease is absent in thepresence of the null vector (pSV3-neo). In addition, there is no effecton the calcium response to the ligands, indicating that the decrease inthe membrane potential response cannot be attributed to altering thecalcium concentration.

While various embodiments of the present invention have been describedabove, it should be understood that they have been presented by way ofexample only, and not limitation. It will be apparent to persons skilledin the relevant art that various changes in form and detail can be madetherein without departing from the spirit and scope of the invention.Thus, the breadth and scope of the present invention should not belimited by any of the above-described exemplary embodiments, but shouldbe defined only in accordance with the following claims and theirequivalents. All publications, patents and patent applications citedherein are incorporated by reference in their entirety into thedisclosure.

1-14. (canceled)
 15. A high throughput screening assay for determiningwhether a test compound is a TRPM5 ion channel-specific modulatorcomprising: (a) contacting a cell that expresses TRPM5 and has beenpreloaded with a membrane potential fluorescent dye, with a testcompound in the presence of potassium chloride; (b) using an opticaldetector, measuring the fluorescent intensity of said cell in thepresence of said potential modulating compound; (c) comparing themeasured fluorescent intensity determined in step (b) to the fluorescentintensity of a different cell that expresses TRPM5 and has beenpreloaded with a membrane potential fluorescent dye, in the presence ofpotassium chloride and the absence of the test compound; and (d)evaluating whether the test compound may be a TRPM5-specific modulatorby determining if the ratio of the fluorescent intensity with potassiumchloride and the test compound to the intensity with potassium chloridein the absence of the test compound is less than or greater than
 1. 16.The assay of claim 15, further comprising selecting a test compound thatenhances TRPM5 activity.
 17. The assay of claim 15, further comprisingselecting a test compound that inhibits TRPM5 activity.
 18. The assay ofclaim 15, wherein said cells are located in a multi-well vessel.
 19. Theassay of claim 18, wherein said multi-well vessel comprises up to 96wells.
 20. The assay of claim 18, wherein said multi-well vesselcomprises greater than 96 wells.
 21. The assay of claim 18, wherein saidmulti-well vessel comprises 384 wells.
 22. The assay of claim 18,wherein said multi-well vessel comprises 1536 wells. 23-26. (canceled)27. The assay of claim 15, wherein said membrane potential fluorescentdye is a Fluorescent Imaging Plate Reader Membrane Potential (FMP) dye.28. The assay of claim 15, wherein said optical detector is selectedfrom the group consisting of: Fluorescent Imaging Plate Reader (FLIPR®),FLEXStation, Voltage/Ion Probe Reader (VIPR), fluorescent microscope andcharge-coupled device (CCD) camera, and Fathway HT.
 29. The assay ofclaim 28, wherein said optical detector is a FLIPR®. 30-63. (canceled)64. The assay of claim 15, wherein said cell of step (a) is a cellselected from the group consisting of: CHO, COS-7, HeLa, HEK 293, PC-12,and BAF.
 65. The assay of claim 64, wherein said cell is a CHO cell. 66.The assay of claim 64, wherein said cell is a HEK 293 cell.
 67. Theassay of claim 15, wherein the amount of said test compound thatcontacts the cell in step (a) is between 0.1 and 1000 μM.
 68. The assayof claim 15, wherein the test compound is a small organic compoundhaving a molecular weight of more than 100 and less than about 10,000Daltons.
 69. The assay of claim 15, wherein the test compound isselected from the group consisting of: synthetic organic compounds,chemical compounds, naturally occurring products, polypeptides,peptides, and nucleic acids.
 70. The assay of claim 15, wherein saidmembrane potential fluorescent dye is a voltage-sensitive dye selectedfrom the group consisting of: modified bisoxonol dyes, sodium dyes,potassium dyes, and thorium dyes.
 71. The assay of claim 15, whereinsaid membrane potential fluorescent dye is a dual wavelength FRET-baseddye selected from the group consisting of: DiSBAC2, DiSBAC3, andCC-2-DMPE.
 72. The assay of claim 15, wherein said optical detector is aFLIPR-Tetra™.